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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744824Generated: November 1, 2026

Methanesulfonyl chloride → HCID 15428650, compound

https://huagongshe.com/reaction/1744824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 15428649HCID 15428649—
SolventPyridineHCID 1049—
ProductHCID 15428650HCID 15428650—

Reaction Steps

A solution of 4-(4-fluorophenyl)-5-(4-pyridinyl)-1H-pyrazol-3-amine prepared as set forth in Example 2 (200 mg, 0.77 mmol) and methanesulfonyl chloride (90 mg) in pyridine (5 ml) was stirred at room temperature overnignt. The pyridine was removed in vacuo and the residue was treated with methylene chloride and water. The resultant precipitate was filtered to give N-[4(4-fluorophenyl)-5-(4-pyridinyl)-1H-pyrazol-3-yl]methanesulfonamide. Additional N-[4(4-fluorophenyl)-5-(4-pyridinyl)-1H-pyrazol-3-yl]methanesulfonamide was contained in the methylene chloride layer. The methylene chloride was stripped in vacuo and the residue purified by chromatography on silica gel using mixtures of ethyl acetate and methanol as eluents. The purified N-[4(4-fluorophenyl)-5-(4-pyridinyl)-1H-pyrazol-3-yl]methanesulfonamide had m.p. 168–170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019005B2
Source datasetuspto-grants-2006_03
ORD IDord-b7bdf25aa7114bbd9128a520fcb2ba09
Source noteuspto-grants-2006_03